Clinical Research Associate

LLRI - Learning Labb Research Institute; Bengaluru; On-site; INR 300,000 - 500,000; Full time

Job summary

LLRI - Learning Labb Research Institute invites applications for an entry-level Clinical Research Associate based in Bengaluru. The role involves monitoring trial sites, verifying data quality, and ensuring GCP compliance and patient safety across assigned studies.

Fresh graduates with degrees in Life Sciences or pharmacy and a willingness to learn are welcome; on-the-job training will be provided.

Qualifications

• Freshers with the right educational background are encouraged to apply.
• On-the-job training will be provided.
• Fresher / 0-1 year experience preferred.

Responsibilities

• Support and conduct site visits for study initiation, monitoring and close-out.
• Verify source documents against CRFs for data accuracy.
• Ensure trials are conducted per GCP, ICH guidelines and study protocol.
• Track patient enrolment and informed consent process.
• Coordinate with investigators, CRO and sponsor teams on trial timelines.
• Support adverse event reporting and patient safety documentation.
• Maintain TMF documentation and site files.

Skills

Clinical Research

GCP Compliance

Patient Safety

Data Quality

Site Monitoring

Education

B.Pharm/BDS/Life Sciences

PG Diploma in Clinical Research

Tools

MS Excel

MS Word

MS PowerPoint

Job description

An entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality and

ensure GCP compliance and patient safety across assigned studies.

Key Responsibilities

• Support and conduct site visits for study initiation, monitoring and close-out
• Verify source documents against Case Report Forms (CRFs) for data accuracy
• Ensure clinical trials are conducted as per GCP, ICH guidelines and study protocol
• Track patient enrolment, informed consent process and protocol adherence
• Coordinate with investigators, CRO and sponsor teams on trial timelines
• Support adverse event reporting and patient safety documentation
• Maintain Trial Master File (TMF) documentation and site files

Must-Have Keywords

Clinical Research | Clinical Trials | GCP Compliance | Patient Safety | Clinical Trial Management

Additional / Good-to-Have Keywords

CRO | Data Quality | Pharmaceutical | Life Sciences | Research | Healthcare

Educational Qualification

B.Pharm/M.Pharm, B.Sc/M.Sc Life Sciences, BDS, BPT, or PG Diploma in Clinical Research.

Experience Required

Fresher / 0-1 year. Freshers with the right educational background and a willingness to learn are

strongly encouraged to apply. On-the-job training will be provided.

Good to Have

• Basic knowledge of MS Office (Word, Excel, PowerPoint)
• Good written and verbal communication skills
• Attention to detail and documentation discipline
• Willingness to learn and work in a regulated, compliance-driven environment